Pyrinuron

Pyrinuron
Names
	IUPAC name 3-(4-Nitrophenyl)-1-(pyridin-3-ylmethyl)urea
	Other names Pyriminil; Vacor
Identifiers
CAS Number	53558-25-1 ;
3D model (JSmol)	Interactive image;
ChemSpider	37276 ;
ECHA InfoCard	100.053.279
PubChem CID	40813;
UNII	Q7BGS137YP ;
CompTox Dashboard (EPA)	DTXSID1042360 ;
	InChI InChI=1S/C13H12N4O3/c18-13(15-9-10-2-1-7-14-8-10)16-11-3-5-12(6-4-11)17(19)20/h1-8H,9H2,(H2,15,16,18) Key: CLKZWXHKFXZIMA-UHFFFAOYSA-N ; InChI=1/C13H12N4O3/c18-13(15-9-10-2-1-7-14-8-10)16-11-3-5-12(6-4-11)17(19)20/h1-8H,9H2,(H2,15,16,18) Key: CLKZWXHKFXZIMA-UHFFFAOYAA;
	SMILES [O-][N+](=O)c1ccc(cc1)NC(=O)NCc2cccnc2;
Properties
Chemical formula	C13H12N4O3
Molar mass	272.264 g·mol−1
Hazards
Main hazards	Toxic
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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	Infobox references

Pyrinuron (Pyriminil, Vacor) is a chemical compound formerly used as a rodenticide.[1] Commercial distribution was voluntarily suspended in 1979 and it is not approved by the Environmental Protection Agency for use in the United States.[2] If it is ingested by humans in high doses, it may selectively destroy insulin-producing beta cells in the pancreas causing type 1 diabetes.[2]

References

Vogel, R. P. (1982). "Poisoning with Vacor Rodenticide". Archives of Pathology and Laboratory Medicine. 106 (3): 153. PMID 6895844.
"Pyriminil". Pyriminil. U.S. National Library of Medicine. Archived from the original on 2013-07-04. Retrieved 2013-11-04.

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[1] Vogel, R. P. (1982). "Poisoning with Vacor Rodenticide". Archives of Pathology and Laboratory Medicine. 106 (3): 153. PMID 6895844.

[hazmap-2] "Pyriminil". Pyriminil. U.S. National Library of Medicine. Archived from the original on 2013-07-04. Retrieved 2013-11-04.